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Effective Date: 01/12/2005 |
Title: Speech Generating Devices
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Revision Date: 12/01/2017
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Document: BI090:00
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CPT Code(s): 92605-92609, E2500, E2502, E2504, E2506, E2508, E2510-E2512, E2599
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Public Statement
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Effective Date:
a)
This policy
will apply to all services performed on or after the above revision date which
will become the new effective date.
b)
For all
services referred to in this policy that were performed before the revision
date, contact customer service for the rules that would apply.
When
a Speech Generating Device is covered under a QualChoice plan, both the device
and the evaluation and services related to the device require preauthorization.
Speech Generating Devices are electronic devices which produce synthesized or
prerecorded speech or other forms of verbal (perhaps written rather than spoken)
communication in response to input from the patient. Vibrators and other noise
producers designed to substitute for vocal cords in allowing a laryngectomized
individual to articulate speech are not considered in this category, and are
covered as DME. Speech Generating Devices are not covered under most QualChoice
plans. Refer to your Summary Plan Description, Certificate of Coverage, or
Explanation of Coverage.
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Medical Statement
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QualChoice may not cover
speech generation devices. For plans where these devices
are covered,
preauthorization of both the device and services related to the device are
required. The following
medical necessity criteria apply and the member should meet
ALL of the following
criteria:
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Prior to the delivery
of the Speech Generating Device (SGD), the patient has had a formal
evaluation of their cognitive and language abilities by a speech-language
pathologist (SLP). The formal, written evaluation must include, at a
minimum, ALL of the following elements:
a.
Evaluation
of current communication impairment, including the type, severity, language
skills, cognitive ability, and anticipated course of the impairment;
b.
An
assessment of whether the individual`s daily communication needs could be met
using natural modes of communication;
c.
A
description of the functional communication goals expected to be achieved and
treatment options;
d.
Rationale
for selection of a specific device and accessories;
e.
A treatment
plan that includes a training schedule for the selected device;
f.
Demonstration that the patient possesses the cognitive and physical abilities to
effectively use the selected device and any accessories to communicate;
g.
For a
subsequent upgrade to a previously issued SGD, information regarding the
functional benefit to the patient of the upgrade compared to the initially
provided SGD; AND
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The patient`s medical
condition is one resulting in a permanent severe expressive speech
disability; and
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The patient`s
speaking needs cannot be met using natural communication methods; and
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Other forms of
treatment have been considered and ruled out; and
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The patient`s speech
disability will benefit from the device ordered; and
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A copy of the Speech
and Language Pathologist`s (SLP) written evaluation and recommendation have
been forwarded to the patient`s treating physician prior to ordering the
device; and
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The SLP performing
the patient evaluation may not be an employee or have a financial
relationship with the supplier of the SGD.
Codes
Used In This BI:
92605 |
Ex
for non-speech device rx |
92606 |
Non-speech device service |
92607 |
Ex
for speech device rx 1hr |
92608 |
Ex
for speech device rx add`l |
92609 |
Use
of speech device service |
E2500 |
Speech gen device, digitized speech, using prerecorded messages, less
than or equal to 8 mins. |
E2502 |
Speech gen device, digitized speech, using prerecorded messages, greater
than 8 mins. but less than or equal to 20 mins. |
E2504 |
Speech gen device, digitized speech, using prerecorded messages, greater
than 20 mins. but less than or equal to 40 mins. |
E2506 |
Speech gen device, digitized speech, using prerecorded messages, greater
than 40 mins. |
E2508 |
Speech gen device, synthesized speech, requiring message formulation by
spelling and access by physical contact with the device |
E2510 |
Speech gen device, synthesized speech, permitting multiple methods of
message formulation and multi methods of device access |
E2511 |
Speech generating software program, for personal computer or personal
digital assistant |
E2512 |
Accessory for speech generating device, mounting system |
E2599 |
Accessory for speech generating device, not otherwise classified |
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Limits
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1.
Laptop
computers, desktop computers, personal digital assistants (PDAs), or other
devices that are not dedicated SGDs are not covered because they do not meet the
definition of durable medical equipment.
2.
Communication aids that do not generate speech are not covered. Communication
aids that are not SGDs are not considered prosthetics for speech, as they do not
replace internal or external body parts lost or impaired by disease or injury.
Examples of non-covered communication aids include the following: picture books;
flashcards; Braille typewriters; TTY (text telephone or TDD) devices; devices
that allow the patient to communicate messages to others with writing (e.g., a
display screen or printout) rather than with synthesized speech; and devices
that allow the user to communicate with a computer rather than with another
person. Although communication aids that do not generate (synthesize) speech may
be useful to patients who otherwise cannot communicate, they do not meet the
definition of a prosthetic device under QualChoice plans.
3.
Any
software, interfaces, cables, adapters, interconnects, and switches necessary
for an accessory to interface with the Speech Generating Device are not covered.
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Background
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Speech generating devices (SGDs) are speech aids that provide individuals with
severe speech impairment the ability to meet their functional speaking needs.
Digitized speech sometimes referred to as devices with "whole message" speech
output, use words, or phrases that have been recorded by an individual other
than the SGD user for playback upon command of the SGD user.
Synthesized speech, unlike prerecorded messages of digitized speech, is a
technology that translates a user`s input into device-generated speech using
algorithms representing linguistic rules. Users of synthesized speech SGDs are
not limited to pre-recorded messages but rather can independently create
messages as their communication needs dictate. Some SGDs require message
formulation by spelling and access by physical contact with a keyboard, touch
screen, or other display containing letters.
Speech generating software programs enable a laptop computer, desktop computer,
or personal digital assistant (PDA) to function as an SGD. Within this policy,
the term SGD also describes these speech generating software programs. Speech
generating devices may permit multiple methods of message formulation and
multiple methods of device access. For purposes of this policy, a SGD with
multiple methods of message formulation should include message selection by two
or more of the following methods: letters, words, pictures, and symbols. A SGD
with multiple methods of access should include the capability to access the
device by two or more of the following: direct physical contact with a keyboard
or touch screen, indirect selection techniques and a specialized access device
such as a joystick, head mouse, optical head pointer, light pointer, infrared
pointer, scanning device, or Morse code.
Upgrades of a SGD are subsequent versions of a SGD`s software program or memory
modules that may include enhanced features or other improvements. Mounting
switches are devices necessary to place the SGD, switches, and other access
devices within the reach of the patient. Accessories for SGDs include, but are
not limited to, access devices that enable selection of letters, words, or
symbols via direct or indirect selection techniques. Examples of access devices
include, but are not limited to, optical head pointers, joysticks, and SGD
scanning devices. The assessment of need for an SGD should be performed by a
qualified speech-language pathologist (SLP). For purposes of this policy, SLPs
are licensed health professionals trained in the diagnosis and treatment of
speech and language disorders. The SLP should hold a Certificate of Clinical
Competence from the American Speech and Hearing Association.
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Reference
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Poole CJ, Millman A.
ABC of medical computing. Adaptive computer technology. Br Med J. 1995;
311(7013):1149-1151.
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Pehringer JL.
Assistive devices: technology to improve communication. Otolaryngol Clin
North Am. 1989; 22(1):143-174.
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Redford JB. Assistive
devices. In: Practice of Geriatrics. 3rd Ed. EH Duthie, JR Katz, eds.
Philadelphia, PA: W.B. Saunders Co.; 1998; 173-186.
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Rostron A, Ward S,
Plant R. Computerized augmentative communication devices for people with
dysphasia: design and evaluation. Eur J Discord Commun. 1996; 31(1):11-30.
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Beukelman DR, Mirenda
P. Augmentative and alternative communication: management of severe
communication disorders in children and adults. Baltimore, MD: P.H. Brookes
Publishers.; 1998.
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Lloyd LL, Fuller DR,
Arvidson HH. Augmentative and alternative communication: a handbook of
principles and practices. Boston, MA: Allyn and Bacon; 1997.
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Cigna/Medicare
coverage:
http://www.cignamedicare.com/pdf/dmerc/supman/chapter09/sm09_SGD.pdf
accessed June 15/2004
Addendum:
Effective 12/01/2017:
Clarification added regarding preauthorization of both device and related
services
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Application to Products
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This policy applies to all health plans administered by QualChoice, both those insured by QualChoice and those that are self-funded by the sponsoring employer, unless there is indication in this policy otherwise or a stated exclusion in your medical plan booklet. Consult the individual plan sponsor Summary Plan Description (SPD) for self-insured plans or the specific Evidence of Coverage (EOC) for those plans insured by QualChoice. In the event of a discrepancy between this policy and a self-insured customer’s SPD or the specific QualChoice EOC, the SPD or EOC, as applicable, will prevail. State and federal mandates will be followed as they apply.
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Changes: QualChoice reserves the right to alter, amend, change or supplement benefit interpretations as needed.
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